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WHAT WE DO

Raising awareness and funds for individuals living with Cystic Fibrosis.

OUR EVENTS

From fundraising galas to exhibition golf matches, we hold a variety of fundraisers throughout the community.

OUR PROGRAMS

Learn more about the LBFs programs and how to apply.

HOW TO HELP

Volunteers and donations help make our Foundation a success! Find out more ways you can help.

FACES OF LBF

Find more about Cystic Fibrosis and some of the amazing individuals we have helped.

MISSION STATEMENT

The Living Breath Foundation is a non-profit organization created to help those living with Cystic Fibrosis.

We award scholarships to qualifying individuals who wish to further their education beyond the high school level. We also assist individuals and families with the added expenses associated with having Cystic Fibrosis, which include the extensive costs of prescription medication and medical equipment. In certain situations, we provide financial assistance for individuals who have prolonged or frequent absences from work.

In addition to providing financial assistance, The Living Breath Foundation plans on producing new and inventive ways to raise awareness about the disease and what it takes to live with the illness.